We're looking for a Senior Engineer, working in the Pharmaceuticals & Medical Products industry in Dublin, California, United States.
Write test protocols and perform V&V and IQOQ testing on developed test fixtures which are controlled with software written in C#, Perl, and PowerShell.
Provide visibility of test development projects regarding schedule, budget, and resources to ensure all stakeholders are aware of timing and help needed to meet critical milestones on time and within budget.
Validate the test fixtures on the production line to ensure that all testing stations are working in proper condition upon release.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
BSEE, BSET or AS degree and equivalent experience
10 years of experience in manufacturing test or engineering within a NPI environment, preferably with medical devices or other highly-regulated electro-mechanical products
Ability to read and understand electrical schematics
Solid electro-mechanical, analog & digital debug and trouble-shooting skill set
Test fixture project management experience with test automation background is strongly desired
Recent experience developing automated test equipment and software using C #, Visual Basic, Visual C++, Perl scripting
Powershell, Labview, LabWindows and/or TestStand experience is desirable
Recent & relevant experience with definition and implementation of production test methods for electromechanical devices and upgrades
Good communications, project management, and technical documentation skills
Strong working knowledge of Microsoft Word and Excel is required
Sufficient hardware experience to build and configure workstations, understand the subsystems and their interactions in an overall system
Experienced in implementing test processes on projects, write test plans/cases, procedures and scripts, and analyzing test results
Must work well in a team environment, be highly motivated, and willing to learn new skills
Good communications and documentation skills, including experience in writing SOPs, work instructions, training and other relevant documentation
Experience working with manufacturing, development and production teams or groups
Previous experience with testing in a medical device manufacturing environment subject to FDA compliance is a plus
The pay range we're offering is 55 - 80 per hour. This position may present an opportunity to go permanent.
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.